Canonical Allele Identifier: PA2829445852
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 661657
ClinVar RCV Id: RCV000819126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp26288Asn
CA349407130
NM_003319.4:c.78862G>A